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rs121908903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908903(C;C)
Make rs121908903(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position112069555
GeneWISP3
is asnp
is mentioned by
dbSNPrs121908903
ebirs121908903
HLIrs121908903
Exacrs121908903
Varsomers121908903
Maprs121908903
PheGenIrs121908903
hapmaprs121908903
1000 genomesrs121908903
hgdprs121908903
ensemblrs121908903
gopubmedrs121908903
geneviewrs121908903
scholarrs121908903
googlers121908903
pharmgkbrs121908903
gwascentralrs121908903
openSNPrs121908903
23andMers121908903
23andMe allrs121908903
SNP Nexus

SNPshotrs121908903
SNPdbers121908903
MSV3drs121908903
GWAS Ctlgrs121908903
Max Magnitude0
OMIM603400
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121908903(C;C)
Alt rs121908903(C;C)
Reference rs121908903(T;T)
Significance Pathogenic
Disease Progressive pseudorheumatoid dysplasia
Variation info
Gene WISP3
CLNDBN Progressive pseudorheumatoid dysplasia
Reversed 0
HGVS NC_000006.11:g.112390758T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006760.4,